Literature DB >> 30263237

A phenyl lipid alkaloid and flavone C-diglucosides from Spergularia marina.

Jeong-Yong Cho1,2, Min-Su Kim1, Yu Geon Lee1, Hang Yeon Jeong1, Hyoung Jae Lee1, Kyung-Sik Ham2, Jae-Hak Moon1.   

Abstract

A phenyl lipid alkaloid and seven phenolic compounds were isolated from the aerial part of Spergularia marina, a halophyte that grows on salt marshes and tidal flat. These compounds were identified as 2,4-di-tert-butylphenol, N-hexacosanoylanthranilic acid, tryptophan, 4-hydroxybenzyol glucopyranoside, luteolin 6-C-β-D-glucopyranoside 8-C-β-D-(2-O-feruloyl)glucopyranoside, luteolin 6-C-β-D-(2-O-feruloyl)glucopyranoside 8-C-β-D-glucopyranoside, apigenin 6-C-β-D-glucopyranoside 8-C-β-D-(2-O-feruloyl)glucopyranoside, and apigenin 6-C-β-D-(2-O-feruloyl)glucopyranoside 8-C-β-D-glucopyranoside. The structures were determined by nuclear magnetic resonance and electrospray ionization-mass spectroscopy.

Entities:  

Keywords:  N-hexacosanoylanthranilic acid; Spergularia marina; flavone C-diglycoside; halophyte; phenolics

Year:  2016        PMID: 30263237      PMCID: PMC6049386          DOI: 10.1007/s10068-016-0009-7

Source DB:  PubMed          Journal:  Food Sci Biotechnol        ISSN: 1226-7708            Impact factor:   2.391


  17 in total

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4.  Structure-antioxidant activity relationships of flavonoids and phenolic acids.

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7.  Purification, characterization, and in vitro activity of 2,4-Di-tert-butylphenol from Pseudomonas monteilii PsF84: conformational and molecular docking studies.

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8.  Antioxidant activities of some tryptophan metabolites: possible implication for inflammatory diseases.

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  2 in total

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Review 2.  Natural Sources and Bioactivities of 2,4-Di-Tert-Butylphenol and Its Analogs.

Authors:  Fuqiang Zhao; Ping Wang; Rima D Lucardi; Zushang Su; Shiyou Li
Journal:  Toxins (Basel)       Date:  2020-01-06       Impact factor: 4.546

  2 in total

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